EP 1354875 A1 20031022 - Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril
Title (en)
Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril
Title (de)
Verfahren zur Synthese von (2S,3aS,7aS)-Perhydroindol-2-carbonsäure und seiner Estern, und Verwendung in der Synthese von Perindopril
Title (fr)
Nouveau procédé de synthèse de l'acide (2S, 3aS, 7aS)-perhydroindole-2-carboxilique et de ses esters, et application à la synthèse du perindopril
Publication
Application
Priority
EP 03291157 A 20030519
Abstract (en)
Preparation of (2S, 3aS, 7aS)-perhydroindole-2-carboxylic acid (I) and its esters (I) is new. Preparation of (2S, 3aS, 7aS)-perhydroindole-2-carboxylic acid (I) and its esters by condensation of (2-oxocyclohexyl) acetic acid (III) with (S)-phenyl glycinol (IV) to form the tricyclic lactam (V) as a diastereoisomeric salt. (V) is then reduced in the presence of a Lewis acid to form (VI) and the 2-hydroxy-1-phenyl group removed to form (VII). Reaction of (VII) with triflic anhydride or an alkylating agent leads to the formation of (VIII). Compounds of formula (VIII) then undergo cyanation to form (IX), which is hydrolyzed to form (X). R = H, benzyl, or 1-6C alkyl; and R1 = trimethylsulfonate or 1-6C alkyl. Independent claims are included for the following: (1) Intermediates of formula (IX) and (X); and (2) Preparing perindopril using (I) prepared by the new process.
Abstract (fr)
Procédé de synthèse industrielle de dérivés de formule (I) : <IMAGE> dans laquelle R représente un atome d'hydrogène ou un groupement benzyle ou alkyle (C1-C6) linéaire ou ramifié, ainsi que leurs sels d'addition à un acide ou à une base minéral(e) ou organique. Application à la synthèse du perindopril et de ses sels pharmaceutiquement acceptables.
IPC 1-7
IPC 8 full level
C07D 209/42 (2006.01)
IPC 8 main group level
C07K 5/00 (2006.01)
CPC (source: EP)
C07D 209/42 (2013.01)
Citation (search report)
- [A] EP 0308339 A1 19890322 - ADIR [FR]
- [A] VINCENT M ET AL: "Stereoselective Synthesis of a New Perhydroindole Derivative of Chiral Iminodiacid, a Potent Inhibitor of Agiotensin Converting Enzyme", TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol. 23, no. 16, 1982, pages 1677 - 1680, XP002155080, ISSN: 0040-4020
Designated contracting state (EPC)
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT RO SE SI SK TR
DOCDB simple family (publication)
EP 1354875 A1 20031022; EP 1354875 B1 20041124; AR 044392 A1 20050914; AT E283258 T1 20041215; DE 60300168 D1 20041230; DE 60300168 T2 20051201; DK 1354875 T3 20050314; ES 2233914 T3 20050616; MY 136639 A 20081128; PT 1354875 E 20050331; SI 1354875 T1 20050228; WO 2004103969 A1 20041202
DOCDB simple family (application)
EP 03291157 A 20030519; AR P040101725 A 20040519; AT 03291157 T 20030519; DE 60300168 T 20030519; DK 03291157 T 20030519; ES 03291157 T 20030519; FR 2004001225 W 20040519; MY PI20041884 A 20040519; PT 03291157 T 20030519; SI 200330011 T 20030519